Canonical Allele Identifier: CA1562881836

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745073T= , CM000667.2:g.90745073T=	GRCh38
NC_000005.9:g.90040890T= , CM000667.1:g.90040890T=	GRCh37
NC_000005.8:g.90076646T=	NCBI36
NG_007083.1:g.191274T=
NG_007083.2:g.220730T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10577T= MANE Select	ENSP00000384582.2:p.Met3526=
ENST00000639431.1:c.265+68864T=	ENSP00000491057.1:n.265+68864T=
ENST00000640374.1:n.3721T=
ENST00000640464.1:n.996T=
ENST00000405460.6:c.10577T=	ENSP00000384582.2:p.Met3526=
ENST00000509621.1:c.3274T=
NM_032119.3:c.10577T=	NP_115495.3:p.Met3526=
NR_003149.1:n.10590T=
XM_011543675.1:c.10574T=	XP_011541977.1:p.Met3525=
XM_011543676.1:c.10496T=	XP_011541978.1:p.Met3499=
XM_011543677.1:c.7880T=	XP_011541979.1:p.Met2627=
XM_011543678.1:c.10577T=	XP_011541980.1:p.Met3526=
XM_011543679.1:c.10577T=	XP_011541981.1:p.Met3526=
NM_032119.4:c.10577T= MANE Select	NP_115495.3:p.Met3526=
XM_017009963.2:c.10598T=	XP_016865452.1:p.Met3533=
XM_017009964.2:c.10595T=	XP_016865453.1:p.Met3532=
XM_017009965.1:c.10595T=	XP_016865454.1:p.Met3532=
XM_017009966.2:c.10517T=	XP_016865455.1:p.Met3506=
XM_017009967.1:c.10502T=	XP_016865456.1:p.Met3501=
XM_017009968.2:c.10598T=	XP_016865457.1:p.Met3533=
XM_017009969.2:c.10598T=	XP_016865458.1:p.Met3533=
XM_017009970.2:c.10598T=	XP_016865459.1:p.Met3533=
XM_017009971.2:c.10598T=	XP_016865460.1:p.Met3533=
XM_017009972.1:c.3716T=	XP_016865461.1:p.Met1239=
XM_017009973.1:c.3695T=	XP_016865462.1:p.Met1232=
XM_017009974.2:c.10598T=	XP_016865463.1:p.Met3533=
NR_003149.2:n.10593T=